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The GMP Operations Coordinator supports daily operations in a GMP manufacturing facility, ensuring supplies and equipment are available, coordinating logistics, and maintaining compliance with regulatory standards while assisting in production runs and quality management.

The Junior Engineer will build, maintain, and scale custom bioreactor systems for cell culture, focusing on assembly, troubleshooting, and process improvement in a laboratory setting.

Lead analytical development and product quality strategy for RTR242, ensuring compliance and quality in small molecule drug development. Collaborate with external partners and cross-functional teams, oversee method development and regulatory interactions. Achieve high standards in manufacturing and QC activities for neurodegenerative disease therapies.

Retro is seeking to build a team for developing therapies targeting aging through cellular reprogramming and autophagy. Interested candidates can apply to express interest in future openings.

The Senior Manager of Quality Operations will oversee day-to-day QA processes, ensure compliance in clinical manufacturing, improve QMS, and support regulatory inspections and audits.

The Scientist role focuses on optimizing differentiation protocols for iHSC production from iPSCs, ensuring reproducibility and scalability, while collaborating across teams and maintaining high standards of documentation.

As a Scientist in Genomics, you will design and optimize genomics experiments, build custom platforms, handle cell cultures, and collaborate with engineering experts to drive research focused on aging-related therapies.